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191 related items for PubMed ID: 3177467

  • 1. Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2).
    Sutherland GR, Gedeon AK, Haan EA, Woodroffe P, Mulley JC.
    Am J Med Genet; 1988; 30(1-2):493-508. PubMed ID: 3177467
    [Abstract] [Full Text] [Related]

  • 2. Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.
    Martínez F, Tomás M, Millán JM, Fernández A, Palau F, Prieto F.
    J Med Genet; 1998 Apr; 35(4):284-7. PubMed ID: 9598720
    [Abstract] [Full Text] [Related]

  • 3. Localisation of the MRX3 gene for non-specific X linked mental retardation.
    Gedeon A, Kerr B, Mulley J, Turner G.
    J Med Genet; 1991 Jun; 28(6):372-7. PubMed ID: 1870093
    [Abstract] [Full Text] [Related]

  • 4. An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.
    Rajab A, Yoo SY, Abdulgalil A, Kathiri S, Ahmed R, Mochida GH, Bodell A, Barkovich AJ, Walsh CA.
    Am J Med Genet A; 2006 Jul 15; 140(14):1504-10. PubMed ID: 16761294
    [Abstract] [Full Text] [Related]

  • 5. Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
    Kozák L, Chiurazzi P, Genuardi M, Pomponi MG, Zollino M, Neri G.
    J Med Genet; 1993 Oct 15; 30(10):866-9. PubMed ID: 8230164
    [Abstract] [Full Text] [Related]

  • 6. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.
    Suthers GK, Turner G, Mulley JC.
    Am J Med Genet; 1988 Oct 15; 30(1-2):485-91. PubMed ID: 3177466
    [Abstract] [Full Text] [Related]

  • 7. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN.
    Am J Med Genet; 1988 Oct 15; 43(1-2):436-42. PubMed ID: 1605223
    [Abstract] [Full Text] [Related]

  • 8. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.
    Strain L, Wright AF, Bonthron DT.
    J Med Genet; 1997 Jul 15; 34(7):535-40. PubMed ID: 9222959
    [Abstract] [Full Text] [Related]

  • 9. MRX8: an X-linked mental retardation condition with linkage to Xq21.
    Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE.
    Am J Med Genet; 1997 Jul 15; 43(1-2):467-74. PubMed ID: 1605227
    [Abstract] [Full Text] [Related]

  • 10. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
    Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE.
    Am J Hum Genet; 1990 Sep 15; 47(3):454-8. PubMed ID: 2393020
    [Abstract] [Full Text] [Related]

  • 11. X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.
    Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C.
    Clin Genet; 1994 Mar 15; 45(3):145-53. PubMed ID: 8026106
    [Abstract] [Full Text] [Related]

  • 12. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.
    Arveiler B, Alembik Y, Hanauer A, Jacobs P, Tranebjaerg L, Mikkelsen M, Puissant H, Piet LL, Mandel JL.
    Am J Med Genet; 1988 Mar 15; 30(1-2):473-83. PubMed ID: 3177465
    [Abstract] [Full Text] [Related]

  • 13. Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.
    Hu LJ, Blumenfeld-Heyberger S, Hanauer A, Weissenbach J, Mandel JL.
    Am J Med Genet; 1994 Jul 15; 51(4):569-74. PubMed ID: 7943041
    [Abstract] [Full Text] [Related]

  • 14. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
    Carpenter NJ, Qu Y, Curtis M, Patil SR.
    Am J Med Genet; 1999 Jul 30; 85(3):230-5. PubMed ID: 10398234
    [Abstract] [Full Text] [Related]

  • 15. New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum.
    Proud VK, Levine C, Carpenter NJ.
    Am J Med Genet; 1999 Jul 30; 43(1-2):458-66. PubMed ID: 1605226
    [Abstract] [Full Text] [Related]

  • 16. A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26.
    Cilliers DD, Parveen R, Clayton P, Cairns SA, Clarke S, Shalet SM, Black GC, Newman WG, Clayton-Smith J.
    Eur J Med Genet; 2007 Jul 30; 50(3):216-23. PubMed ID: 17369115
    [Abstract] [Full Text] [Related]

  • 17. An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness.
    Renier WO, Gabreëls FJ, Jasper HH, Hustinx TW, Geelen JA, van Haelst UJ.
    J Ment Defic Res; 1982 Mar 30; 26(Pt 1):27-40. PubMed ID: 7077653
    [No Abstract] [Full Text] [Related]

  • 18. Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.
    Carpenter NJ, Brown WT, Qu Y, Keenan KL.
    Am J Med Genet; 1999 Jul 30; 85(3):266-70. PubMed ID: 10398241
    [Abstract] [Full Text] [Related]

  • 19. Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.
    Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J.
    Am J Med Genet; 1999 Jul 30; 43(1-2):479-90. PubMed ID: 1605230
    [Abstract] [Full Text] [Related]

  • 20. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM, Penttinen M, von Koskull H.
    Hum Genet; 1992 Nov 30; 90(3):263-6. PubMed ID: 1362558
    [Abstract] [Full Text] [Related]

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